-
2
-
-
0024404351
-
From Podophyllotoxin Glucoside to Etoposide
-
(b) Stähelin, H.; von Wartburg, A. From Podophyllotoxin Glucoside to Etoposide. Prog. Drug. Res. 1989, 33, 169-266.
-
(1989)
Prog. Drug. Res.
, vol.33
, pp. 169-266
-
-
Stähelin, H.1
Von Wartburg, A.2
-
3
-
-
0026011121
-
The Chemical and Biological Route from Podophyllotoxin Glucoside to Etoposide: Ninth Cain Memorial Award Lecture
-
(c) Stähelin, H.; von Wartburg, A. The Chemical and Biological Route from Podophyllotoxin Glucoside to Etoposide: Ninth Cain Memorial Award Lecture. Cancer Res. 1991, 51, 5-15.
-
(1991)
Cancer Res.
, vol.51
, pp. 5-15
-
-
Stähelin, H.1
Von Wartburg, A.2
-
4
-
-
0027330403
-
Podophyllotoxin, Steganacin and Combretastatin, Natural Products that Bind at the Colchicine Site of Tubuline
-
(d) Sackett, D. L. Podophyllotoxin, Steganacin and Combretastatin, Natural Products that Bind at the Colchicine Site of Tubuline. Pharmac. Ther. 1993, 59, 163-228.
-
(1993)
Pharmac. Ther.
, vol.59
, pp. 163-228
-
-
Sackett, D.L.1
-
5
-
-
77049217359
-
The Biological Effects and the Chemical Composition of Podophyllotoxin. A review
-
Kelly, M. G.; Hartwell, J. L. The Biological Effects and the Chemical Composition of Podophyllotoxin. A review, J. Natl. Cancer Inst. 1954, 14, 967-1010.
-
(1954)
J. Natl. Cancer Inst.
, vol.14
, pp. 967-1010
-
-
Kelly, M.G.1
Hartwell, J.L.2
-
6
-
-
15644379380
-
VM 26, a new podophyllotoxin glucoside derivative with anti-L-1210 activity
-
(a) Stahelin, L. VM 26, a new podophyllotoxin glucoside derivative with anti-L-1210 activity. Proc. Am. Assoc. Cancer Res. 1969, 10, 86-86.
-
(1969)
Proc. Am. Assoc. Cancer Res.
, vol.10
, pp. 86-86
-
-
Stahelin, L.1
-
7
-
-
0014827776
-
4′-Demethyl-epipodophyllotixm thenylidene glucoside (VM 26), a Podophyllum Compound with a New Mechanism of Action
-
(b) Stähelin, H. 4′-Demethyl-epipodophyllotixm thenylidene glucoside (VM 26), a Podophyllum Compound with a New Mechanism of Action. Eur. J. Cancer 1970, 6, 303-311.
-
(1970)
Eur. J. Cancer
, vol.6
, pp. 303-311
-
-
Stähelin, H.1
-
8
-
-
0015601539
-
Activity of a New Glycosidic Lignan Derivative (VP 16-213) Related to Podophyllotoxin in Experimental Tumors
-
(c) Stähelin, H. Activity of a New Glycosidic Lignan Derivative (VP 16-213) Related to Podophyllotoxin in Experimental Tumors. Eur. J. Cancer 1973, 9, 215-221.
-
(1973)
Eur. J. Cancer
, vol.9
, pp. 215-221
-
-
Stähelin, H.1
-
9
-
-
0028144889
-
Etoposide: Current Status and Future Perspectives in the Management of Malignant Neoplasms
-
Belani, C. P.; Doyle, L. A.; Aigner, J. Etoposide: Current Status and Future Perspectives in the Management of Malignant Neoplasms. Cancer Chemother. Pharmacol. 1994, 34 (suppl.), S118-S126.
-
(1994)
Cancer Chemother. Pharmacol.
, vol.34
, Issue.SUPPL.
-
-
Belani, C.P.1
Doyle, L.A.2
Aigner, J.3
-
10
-
-
0028144885
-
Pharmacodynamics and Long-Term Toxicity of Etoposide
-
Kobayashi, K.; Ratain, M. J. Pharmacodynamics and Long-Term Toxicity of Etoposide. Cancer Chemother. Pharmacol. 1994, 34 (suppl.), S64-S68.
-
(1994)
Cancer Chemother. Pharmacol.
, vol.34
, Issue.SUPPL.
-
-
Kobayashi, K.1
Ratain, M.J.2
-
11
-
-
0020701027
-
DNA Damage as a Basis for 4′-Demethyl-epipodophyllotoxin-9-(4,6-O-ethylidene-β-D- glucopyranoside) (Etoposide) Cytotoxicity
-
(a) Wozniak, A. J.; Ross, W. E. DNA Damage as a Basis for 4′-Demethyl-epipodophyllotoxin-9-(4,6-O-ethylidene-β-D- glucopyranoside) (Etoposide) Cytotoxicity. Cancer Res. 1983, 43, 120-124.
-
(1983)
Cancer Res.
, vol.43
, pp. 120-124
-
-
Wozniak, A.J.1
Ross, W.E.2
-
12
-
-
0021240783
-
Inhibition of the DNA Catenation Activity of Type II Topoisomerase by VP-16-213 and VM-26
-
(b) Minocha, A.; Long, B. Inhibition of the DNA Catenation Activity of Type II Topoisomerase by VP-16-213 and VM-26. Biochem. Biophys. Res. Commun. 1984, 122, 165-170.
-
(1984)
Biochem. Biophys. Res. Commun.
, vol.122
, pp. 165-170
-
-
Minocha, A.1
Long, B.2
-
13
-
-
0029802613
-
Topoisomerase II Etoposide Interaction Direct the Formation of Drug-induced Enzyme-DNA Cleavage Complexes
-
(c) Burden, D. A.; Kingma, P. S.; Froelich-Ammon, S. J.; Bjornsti, M.-A.; Patchan, M. W.; Thompson, R. B.; Osheroff, N. Topoisomerase II Etoposide Interaction Direct the Formation of Drug-induced Enzyme-DNA Cleavage Complexes. J. Biol. Chem. 1996, 46, 29238-29244.
-
(1996)
J. Biol. Chem.
, vol.46
, pp. 29238-29244
-
-
Burden, D.A.1
Kingma, P.S.2
Froelich-Ammon, S.J.3
Bjornsti, M.-A.4
Patchan, M.W.5
Thompson, R.B.6
Osheroff, N.7
-
14
-
-
0022981124
-
Studies on Lignan Lactone Antitumor Agents. I. Synthesis of Aminoglycosidic Lignan Variants Related to Podophyllotoxin
-
(a) Saito, H.; Yoshikawa, H.; Nishimura, Y.; Kondo, S.; Takeuchi, T.; Umezawa, H. Studies on Lignan Lactone Antitumor Agents. I. Synthesis of Aminoglycosidic Lignan Variants Related to Podophyllotoxin. Chem. Pharm. Bull. 1986, 34, 3733-3740.
-
(1986)
Chem. Pharm. Bull.
, vol.34
, pp. 3733-3740
-
-
Saito, H.1
Yoshikawa, H.2
Nishimura, Y.3
Kondo, S.4
Takeuchi, T.5
Umezawa, H.6
-
15
-
-
0023037509
-
Studies on Lignan Lactone Antitumor Agents. II. Synthesis of N-alkylamino- and 2,6-dideoxy-2-aminoglycosidic Lignan Variants Related to Podophyllotoxin
-
(b) Saito, H.; Yoshikawa, H.; Nishimura, Y.; Kondo, S.; Takeuchi, T.; Umezawa, H. Studies on Lignan Lactone Antitumor Agents. II. Synthesis of N-alkylamino- and 2,6-dideoxy-2-aminoglycosidic Lignan Variants Related to Podophyllotoxin. Chem. Pharm. Bull. 1986, 34, 3741-3746.
-
(1986)
Chem. Pharm. Bull.
, vol.34
, pp. 3741-3746
-
-
Saito, H.1
Yoshikawa, H.2
Nishimura, Y.3
Kondo, S.4
Takeuchi, T.5
Umezawa, H.6
-
16
-
-
0025752255
-
Facile Synthesis of Thioglucose Analogs of the Anticancer Agent, Etoposide
-
(a) Showalter, H. D. H.; Winters, R. T.; Sercel, A. D.; Michel, A. Facile Synthesis of Thioglucose Analogs of the Anticancer Agent, Etoposide. Tetrahedron Lett. 1991, 32, 2849-2852.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 2849-2852
-
-
Showalter, H.D.H.1
Winters, R.T.2
Sercel, A.D.3
Michel, A.4
-
17
-
-
0026061377
-
A Short and Simple Synthesis of the Thioglucose Analogs of the Antitumor Agent, Etoposide
-
(b) Allevi, P.; Anastasia, M.; Ciuffreda, P. A Short and Simple Synthesis of the Thioglucose Analogs of the Antitumor Agent, Etoposide. Tetrahedron Lett. 1991, 32, 6227-6230.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 6227-6230
-
-
Allevi, P.1
Anastasia, M.2
Ciuffreda, P.3
-
18
-
-
0038842487
-
Synthesis of the All Four Possible Diastereoisomers of Etoposide and its Aminoglycosidic Analogues via Optical Resolution of (±)Podophyllotoxin by Glycosidation with D- and L-sugars
-
(c) Saito, H.; Nishimura, Y.; Kondo, S.; Umezawa, H. Synthesis of the All Four Possible Diastereoisomers of Etoposide and its Aminoglycosidic Analogues via Optical Resolution of (±)Podophyllotoxin by Glycosidation with D- and L-sugars. Chem. Lett. 1987, 799-802.
-
(1987)
Chem. Lett.
, pp. 799-802
-
-
Saito, H.1
Nishimura, Y.2
Kondo, S.3
Umezawa, H.4
-
19
-
-
0027437381
-
The First Synthesis of the N-glucosyl Analogues of the Antitumor Agent, Etoposide
-
Allevi, P.; Anastasia, M.; Ciuffreda, P. The First Synthesis of the N-glucosyl Analogues of the Antitumor Agent, Etoposide. Tetrahedron Lett. 1993, 34, 7313-7316.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 7313-7316
-
-
Allevi, P.1
Anastasia, M.2
Ciuffreda, P.3
-
20
-
-
21144463571
-
A Simple Synthesis of C-Glucosides Related to the Antitumor Agent Etoposide
-
Allevi, P.; Anastasia, M.; Ciuffreda, P.; Scala, A. A Simple Synthesis of C-Glucosides Related to the Antitumor Agent Etoposide. J. Carbohydr. Chem. 1993, 12, 209-222.
-
(1993)
J. Carbohydr. Chem.
, vol.12
, pp. 209-222
-
-
Allevi, P.1
Anastasia, M.2
Ciuffreda, P.3
Scala, A.4
-
21
-
-
15644369515
-
Phase I Clinical Trial and Pharmacokinetic Study of the New Etoposide Analog, NK 611 in Patients with Advanced Solid Tumors
-
(a) Kudoh, S.; Fokuoka, M.; Furuse, K.; et al. Phase I Clinical Trial and Pharmacokinetic Study of the New Etoposide Analog, NK 611 in Patients with Advanced Solid Tumors. Ann. Oncol. 1993, 3 (suppl. 1), 146-146.
-
(1993)
Ann. Oncol.
, vol.3
, Issue.SUPPL. 1
, pp. 146-146
-
-
Kudoh, S.1
Fokuoka, M.2
Furuse, K.3
-
22
-
-
0028881109
-
Activity of NK 611, a New Epipodophyllotoxin Derivative, Against Colony Forming Units from Freshly Explanted Human Tumours in Vitro
-
(b) Hanauske, A.-R.; Wüster, K. C.; Lehmer, A.; Rotter, M.; Schneider, P.; Kaeser-Fröhlich, A.; Rastetter, J.; Depenbrock, H. Activity of NK 611, a New Epipodophyllotoxin Derivative, Against Colony Forming Units from Freshly Explanted Human Tumours In Vitro. Eur. J. Cancer 1995, 31A, 1677-1681.
-
(1995)
Eur. J. Cancer
, vol.31 A
, pp. 1677-1681
-
-
Hanauske, A.-R.1
Wüster, K.C.2
Lehmer, A.3
Rotter, M.4
Schneider, P.5
Kaeser-Fröhlich, A.6
Rastetter, J.7
Depenbrock, H.8
-
23
-
-
33845375960
-
Syntheses of 2,3,6-Trideoxy-3-amino- and 2,3,6-Trideoxy-3-nitrohexoses
-
(a) Hauser, F. M.; Ellenberger, S. Syntheses of 2,3,6-Trideoxy-3-amino- and 2,3,6-Trideoxy-3-nitrohexoses. Chem. Rev. 1986, 86, 35-67.
-
(1986)
Chem. Rev.
, vol.86
, pp. 35-67
-
-
Hauser, F.M.1
Ellenberger, S.2
-
25
-
-
0000356472
-
Doxorubicin Anticancer Antibiotics
-
Academic Press; New York
-
Arcamone, F. Doxorubicin Anticancer Antibiotics. Medicinal Chemistry; Academic Press; New York, 1981; Vol. 17.
-
(1981)
Medicinal Chemistry
, vol.17
-
-
Arcamone, F.1
-
27
-
-
0024532176
-
Rationale for the Synthesis and Preliminary Biological Evaluation of Highly Active New Antitumor Nitrosoureido Sugars
-
Roger, P.; Monneret, C.; Fournier, J.-P.; Choay, P.; Gagnet, R.; Gosse, C.; Letourneux, Y.; Atassi, G.; Gouyette, A. Rationale for the Synthesis and Preliminary Biological Evaluation of Highly Active New Antitumor Nitrosoureido Sugars. J. Med. Chem. 1989, 32, 16-23.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 16-23
-
-
Roger, P.1
Monneret, C.2
Fournier, J.-P.3
Choay, P.4
Gagnet, R.5
Gosse, C.6
Letourneux, Y.7
Atassi, G.8
Gouyette, A.9
-
28
-
-
0024341211
-
Characterization of the Anti-Tumour Activity Against Solid Tumours of a New Nitrosoureido Sugar: CY 233
-
(a) Atassi, G.; Dumont, P.; Gosse, C.; Fournier, J.-P.; Gouyette, A.; Roger, P. Characterization of the Anti-Tumour Activity Against Solid Tumours of a New Nitrosoureido Sugar: CY 233. Cancer Chemother. Pharmacol. 1989,25, 205-209.
-
(1989)
Cancer Chemother. Pharmacol.
, vol.25
, pp. 205-209
-
-
Atassi, G.1
Dumont, P.2
Gosse, C.3
Fournier, J.-P.4
Gouyette, A.5
Roger, P.6
-
29
-
-
0025298410
-
Evaluation of a New Nitrosoureido Water-Soluble Sugar, Ecomustine or CY 233 (NSC 609224), on Human Xenografts
-
(b) Dumont, P.; Atassi, G.; Roger, P. Evaluation of a New Nitrosoureido Water-Soluble Sugar, Ecomustine or CY 233 (NSC 609224), on Human Xenografts. In Vivo 1990, 4, 61-64.
-
(1990)
In Vivo
, vol.4
, pp. 61-64
-
-
Dumont, P.1
Atassi, G.2
Roger, P.3
-
30
-
-
37049086929
-
Stereocontrolled route to 3-amino-2,3,6-trideoxy-hexopyranoside. K10 Montmorillonite as a glycosidation reagent for Acosaminide Synthesis
-
Florent, J. C.; Monneret, C. Stereocontrolled route to 3-amino-2,3,6-trideoxy-hexopyranoside. K10 Montmorillonite as a glycosidation reagent for Acosaminide Synthesis. J. Chem. Soc., Chem. Commun. 1987, 1171-1172.
-
(1987)
J. Chem. Soc., Chem. Commun.
, pp. 1171-1172
-
-
Florent, J.C.1
Monneret, C.2
-
31
-
-
0031539026
-
Synthesis of 6-hydroxy-L-daunosamine and L-daunosamine derivatives
-
Daley, L.; Roger, P.; Monneret, C. Synthesis of 6-hydroxy-L-daunosamine and L-daunosamine derivatives. J. Carbohydr. Chem. 1997, 16, 25-48.
-
(1997)
J. Carbohydr. Chem.
, vol.16
, pp. 25-48
-
-
Daley, L.1
Roger, P.2
Monneret, C.3
-
32
-
-
33746173864
-
Anomeric O-alkylation of O-acetyl-Protected Sugars
-
(a) Klotz, W.; Schmidt, R. R. Anomeric O-alkylation of O-acetyl-Protected Sugars. J. Carbohydr. Res. 1994, 13, 1093-1101.
-
(1994)
J. Carbohydr. Res.
, vol.13
, pp. 1093-1101
-
-
Klotz, W.1
Schmidt, R.R.2
-
33
-
-
0000809367
-
Direct O-glycosyl Trichloracetamidate Formation. Nucleophilicity of the Anomeric Oxygen Atom
-
(b) Schmidt, R. R.; Michel, J. Direct O-glycosyl Trichloracetamidate Formation. Nucleophilicity of the Anomeric Oxygen Atom. Tetrahedron Lett. 1984, 25, 821-824.
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 821-824
-
-
Schmidt, R.R.1
Michel, J.2
-
34
-
-
0025847758
-
2-Deoxy-1-O-silylated-β-hexopyranose, Useful Glycosyl Donors and Synthetic Intermediates
-
Priebe, W.; Grynkiewicz, G.; Neamati, N. 2-Deoxy-1-O-silylated-β-hexopyranose, Useful Glycosyl Donors and Synthetic Intermediates. Tetrahedron Lett. 1991, 32, 2079-2082.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 2079-2082
-
-
Priebe, W.1
Grynkiewicz, G.2
Neamati, N.3
-
35
-
-
0025004204
-
Semisynthetic Rhodomycins: Novel Glycosylation Methods for the Synthesis of Anthracycline Oligosaccharides
-
Kolar, C.; Kneissl, G.; Knödler, U.; Dehmel, K. Semisynthetic Rhodomycins: Novel Glycosylation Methods for the Synthesis of Anthracycline Oligosaccharides. Angew. Chem., Int. Ed. Engl. 1990, 29, 809-810.
-
(1990)
Angew. Chem., Int. Ed. Engl.
, vol.29
, pp. 809-810
-
-
Kolar, C.1
Kneissl, G.2
Knödler, U.3
Dehmel, K.4
-
36
-
-
0025007120
-
A New Approach to the Synthesis of Etoposide
-
Kolar, C.; Moldenhauer, H.; Kneissl, G. A New Approach to the Synthesis of Etoposide. J. Carbohydr. Chem. 1990, 9, 571-583.
-
(1990)
J. Carbohydr. Chem.
, vol.9
, pp. 571-583
-
-
Kolar, C.1
Moldenhauer, H.2
Kneissl, G.3
-
37
-
-
84980126260
-
Partial synthesis of 4′-Demethylepidodophyllotoxin
-
(a) Kuhn, M.; Keller-Juslén, C.; von Wartburg, A. Partial synthesis of 4′-Demethylepidodophyllotoxin. Helv. Chim. Acta 1969, 52, 944-947.
-
(1969)
Helv. Chim. Acta
, vol.52
, pp. 944-947
-
-
Kuhn, M.1
Keller-Juslén, C.2
Von Wartburg, A.3
-
38
-
-
0014453173
-
Mitosisinhibiting Substances. Glycosylation Process. II. Glycosides of 4′-Demethylepipodophyllotoxin
-
(b) Kuhn, M.; von Wartburg, A. Mitosisinhibiting Substances. Glycosylation Process. II. Glycosides of 4′-Demethylepipodophyllotoxin. Helv. Chim. Acta 1969, 52, 948-955.
-
(1969)
Helv. Chim. Acta
, vol.52
, pp. 948-955
-
-
Kuhn, M.1
Von Wartburg, A.2
-
39
-
-
0024412180
-
Antitumor Agents. 107. New Cytotoxic 4′-alkylamino analogues of 4′-Demethyl-Epipodophyllotoxin as Inhibitors of Human DNA Topoisomerase II
-
(a) Lee, K.-H.; Imakura, Y.; Haruna, M.; Beers, S. A.; Thurston, L. S.; Dai, H.-J.; Chen, C.-H. Antitumor Agents. 107. New Cytotoxic 4′-alkylamino analogues of 4′-Demethyl-Epipodophyllotoxin as Inhibitors of Human DNA Topoisomerase II. J. Nat. Prod. 1989, 52, 606-611.
-
(1989)
J. Nat. Prod.
, vol.52
, pp. 606-611
-
-
Lee, K.-H.1
Imakura, Y.2
Haruna, M.3
Beers, S.A.4
Thurston, L.S.5
Dai, H.-J.6
Chen, C.-H.7
-
40
-
-
0024504542
-
Antitumors Agents. 100. Inhibition of DNA Topoisomerase II by Cytotoxic Etherane Ester Derivatives of Podophyllotoxin and α-Peltatin
-
(b) Thurston, L. S.; Imakura, Y.; Haruna, M.; Li, D.-H.; Liu, Z.-C.; Liu, S.-Y.; Cheng, Y.-C.; Lee, K. H. Antitumors Agents. 100. Inhibition of DNA Topoisomerase II by Cytotoxic Etherane Ester Derivatives of Podophyllotoxin and α-Peltatin. J. Med. Chem. 1989, 32, 604-608.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 604-608
-
-
Thurston, L.S.1
Imakura, Y.2
Haruna, M.3
Li, D.-H.4
Liu, Z.-C.5
Liu, S.-Y.6
Cheng, Y.-C.7
Lee, K.H.8
-
41
-
-
33646564507
-
Selective O-Demethylation of Catechol Ethers. Comparison of Boron Tribromide and Iodotrimethylsilane
-
Vickery, E. H.; Pahler, L. F.; Eisenbraun, E. J. Selective O-Demethylation of Catechol Ethers. Comparison of Boron Tribromide and Iodotrimethylsilane. J. Org. Chem. 1979, 44, 4444-4446.
-
(1979)
J. Org. Chem.
, vol.44
, pp. 4444-4446
-
-
Vickery, E.H.1
Pahler, L.F.2
Eisenbraun, E.J.3
-
42
-
-
0542430100
-
Quantitative Dealkylation of Alkyl Ethers via Treatment with Trimethylsilyl Iodide. A New Method for Ethers Hydrolysis
-
Jung, M. E.; Lyster, M. A. Quantitative Dealkylation of Alkyl Ethers via Treatment with Trimethylsilyl Iodide. A New Method for Ethers Hydrolysis. J. Org. Chem. 1977, 42, 3761-3764.
-
(1977)
J. Org. Chem.
, vol.42
, pp. 3761-3764
-
-
Jung, M.E.1
Lyster, M.A.2
-
43
-
-
0003686469
-
Synthetic Methods and Reactions. 62. Transformations with Chlorotrimethylsilane/Sodium Iodide, a Convenient in Situ Iodotrimethylsilane Reagent
-
Olah, G. A.; Narang, S. C.; Gupta, B. G. B.; Malhotra, R. Synthetic Methods and Reactions. 62. Transformations with Chlorotrimethylsilane/Sodium Iodide, a Convenient in Situ Iodotrimethylsilane Reagent. J. Org. Chem. 1979, 44, 1247-1251.
-
(1979)
J. Org. Chem.
, vol.44
, pp. 1247-1251
-
-
Olah, G.A.1
Narang, S.C.2
Gupta, B.G.B.3
Malhotra, R.4
-
44
-
-
84985300163
-
Chlorotrimethylsilane/Sodium Iodide: A New Reagent for Conversion of Alcohols into Iodides
-
Morita, T.; Yoshida S.; Okamoto Y.; Sakurai H. Chlorotrimethylsilane/Sodium Iodide: A New Reagent for Conversion of Alcohols into Iodides. Synthesis 1979, 379-379.
-
(1979)
Synthesis
, pp. 379-379
-
-
Morita, T.1
Yoshida, S.2
Okamoto, Y.3
Sakurai, H.4
-
45
-
-
84989438178
-
Synthetic Application of Cyanotrimethylsilane, iodotrimethylsilane, Azidotrimethylsilane and Methylthiomethy/trimethylsilane
-
Groutas, W. C.; Felker D. Synthetic Application of Cyanotrimethylsilane, iodotrimethylsilane, Azidotrimethylsilane and Methylthiomethy/trimethylsilane. Synthesis 1980, 861-868.
-
(1980)
Synthesis
, pp. 861-868
-
-
Groutas, W.C.1
Felker, D.2
-
46
-
-
0025853134
-
Synthesis and Antitumor Activity of Structural Analogues of the Epipodophyllotoxins
-
Klein, L. L.; Yeung, C. M.; Chu, D. T.; McDonald, G. J.; Clement, J. J.; Plattner, J. J. Synthesis and Antitumor Activity of Structural Analogues of the Epipodophyllotoxins. J. Med. Chem. 1991, 34, 984-992.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 984-992
-
-
Klein, L.L.1
Yeung, C.M.2
Chu, D.T.3
McDonald, G.J.4
Clement, J.J.5
Plattner, J.J.6
-
47
-
-
0030989428
-
A one-pot Efficient Synthesis of the Potent Cytotoxic Podophyllotoxin Derivative, NPF
-
32 by further treatment with 4-fluoroaniline instead of barium carbonate; see Daley, L.; Meresse, P.; Bertounesque, E.; Monneret, C. A one-pot Efficient Synthesis of the Potent Cytotoxic Podophyllotoxin Derivative, NPF. Tetrahedron Lett. 1997, 38, 2673-2676.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 2673-2676
-
-
Daley, L.1
Meresse, P.2
Bertounesque, E.3
Monneret, C.4
-
48
-
-
0025350760
-
Antitumor Agents. 111. New 4-Hydroxylated and 4-Halogenated Anilino Derivatives of 4′-Demethylepipodophyllotoxin as Potent Inhibitors of Human DNA Topoisomerase. II
-
Lee, K.-H.; Beers, S. A.; Mori, M.; Wang, Z.-Q.; Kuo, Y.-H.; Li, L.; Liu, S. Y.; Chang, J.-Y.; Han, F. S.; Cheng, Y.-C.; Antitumor Agents. 111. New 4-Hydroxylated and 4-Halogenated Anilino Derivatives of 4′-Demethylepipodophyllotoxin as Potent Inhibitors of Human DNA Topoisomerase. II. J. Med. Chem. 1990, 33, 1364-1368.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 1364-1368
-
-
Lee, K.-H.1
Beers, S.A.2
Mori, M.3
Wang, Z.-Q.4
Kuo, Y.-H.5
Li, L.6
Liu, S.Y.7
Chang, J.-Y.8
Han, F.S.9
Cheng, Y.-C.10
-
49
-
-
0014241902
-
Mitosis-inhibiting Substances. XX. Cleavage of Acyl Protective Groups in Alkali-sensitive Glucosides
-
Kuhn, M.; von Warburg, A. Mitosis-inhibiting Substances. XX. Cleavage of Acyl Protective Groups in Alkali-sensitive Glucosides. Helv. Chim. Acta 1968, 51, 163-168.
-
(1968)
Helv. Chim. Acta
, vol.51
, pp. 163-168
-
-
Kuhn, M.1
Von Warburg, A.2
-
50
-
-
0027936311
-
Structure-activity relationships of VP-16 analogues
-
Long, B. H.; Casazza, A. M. Structure-activity relationships of VP-16 analogues. Cancer Chemother. Pharmacol. 1994, 34, 526-531.
-
(1994)
Cancer Chemother. Pharmacol.
, vol.34
, pp. 526-531
-
-
Long, B.H.1
Casazza, A.M.2
-
51
-
-
0016344556
-
Turbidimetric Studies of the in Vitro Assembly and Disassembly of Porcine Neurotubules
-
Gaskin, F.; Babtor, C. R. Turbidimetric Studies of the In Vitro Assembly and Disassembly of Porcine Neurotubules. J. Mol. Biol. 1974, 89, 737-758.
-
(1974)
J. Mol. Biol.
, vol.89
, pp. 737-758
-
-
Gaskin, F.1
Babtor, C.R.2
-
52
-
-
15644373250
-
Dostatin 10, a powerful cytostatic peptide derived from a marine animal
-
Bai, R.; Pettit, G. R.; Hamel, E. Dostatin 10, a powerful cytostatic peptide derived from a marine animal. Biochem. Pharmacol. 1993, 39, 13560-13565.
-
(1993)
Biochem. Pharmacol.
, vol.39
, pp. 13560-13565
-
-
Bai, R.1
Pettit, G.R.2
Hamel, E.3
-
53
-
-
0015595694
-
Microtubule Assembly in the Absence of Added Nucleophiles
-
Shelansky, M. L.; Gaskin, F.; Cantor, C. R. Microtubule Assembly in the Absence of Added Nucleophiles. Proc. Natl. Acad. Sci. 1973, 70, 765-786.
-
(1973)
Proc. Natl. Acad. Sci.
, vol.70
, pp. 765-786
-
-
Shelansky, M.L.1
Gaskin, F.2
Cantor, C.R.3
-
54
-
-
0027369170
-
The antileukaemic alkaloid fagaronine is an inhibitor of DNA topoisomerases I and II
-
Larsen, A. K.; Grondard, L.; Couprie, J.; Desoize, B.; Comoe, L.; Jardillier, J.-C.; Riou, J.-F. The antileukaemic alkaloid fagaronine is an inhibitor of DNA topoisomerases I and II. Biochem. Pharmacol. 1993, 46, 1403-1412.
-
(1993)
Biochem. Pharmacol.
, vol.46
, pp. 1403-1412
-
-
Larsen, A.K.1
Grondard, L.2
Couprie, J.3
Desoize, B.4
Comoe, L.5
Jardillier, J.-C.6
Riou, J.-F.7
|